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Viscosities, diffusion coefficients, and mixing times of intrinsic fluorescent organic molecules in brown limonene secondary organic aerosol and tests of the Stokes-Einstein equation

机译:棕色柠檬烯二次有机气溶胶中固有荧光有机分子的粘度,扩散系数和混合时间和斯托克斯 - 爱因斯坦方程的试验

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Viscosities and diffusion rates of organics within secondary organic aerosol (SOA) remain uncertain. Using the bead-mobility technique, we measured viscosities as a function of water activity (a(w)) of SOA generated by the ozonolysis of limonene followed by browning by exposure to NH3 (referred to as brown limonene SOA or brown LSOA). These measurements together with viscosity measurements reported in the literature show that the viscosity of brown LSOA increases by 3-5 orders of magnitude as the a w decreases from 0.9 to approximately 0.05. In addition, we measured diffusion coefficients of intrinsic fluorescent organic molecules within brown LSOA matrices using rectangular area fluorescence recovery after photobleaching. Based on the diffusion measurements, as the a w decreases from 0.9 to 0.33, the average diffusion coefficient of the intrinsic fluorescent organic molecules decreases from 5.5 +/- 10(9) to 7.1 +/- 10(13) cm(2) s(1) and the mixing times of intrinsic fluorescent organic molecules within 200 nm brown LSOA particles increases from 0.002 to 14 s. These results suggest that the mixing times of large organics in the brown LSOA studied here are short ( 1 h) for a(w) and temperatures often found in the planetary boundary layer (PBL). Since the diffusion coefficients and mixing times reported here correspond to SOA generated using a high mass loading (similar to 1000 mu gm(3)), biogenic SOA particles found in the atmosphere with mass loadings similar to 10 mu gm(3) are likely to have higher viscosities and longer mixing times (possibly 3 orders of magnitude longer). These new measurements of viscosity and diffusion were used to test the accuracy of the Stokes-Einstein relation for predicting diffusion rates of organics within brown LSOA matrices. The results show that the Stokes-Einstein equation gives accurate predictions of diffusion coefficients of large organics within brown LSOA matrices when the viscosity of the matrix is as high as 10(2) to 10(4)
机译:二次有机气溶胶中有机物(SOA)内有机物的粘度和扩散率仍然不确定。使用珠子迁移率技术,我们测量的粘度作为由柠檬酸臭氧溶解的SOA产生的水活性(A(W))的函数,然后通过暴露于NH 3(称为棕色柠檬烯SOA或棕色LSOA)。这些测量与文献中报道的粘度测量一起表明,棕色LSOA的粘度增加3-5个数量级,因为W从0.9降至约0.05。此外,我们使用光漂白后使用矩形区域荧光回收来测量棕色LSOA基质内固有荧光有机分子的扩散系数。基于扩散测量,随着AW从0.9降低0.9至0.33,内在荧光有机分子的平均扩散系数从5.5 +/- 10(9)〜7.1 +/- 10(13)cm(2)S( 1)和200nm棕色LSOA颗粒内的固有荧光有机分子的混合时间从0.002-14秒增加。这些结果表明,这里研究的棕色LSOA中的大型有机物的混合时间是(w)的短(& 1 h),并且在行星边界层(pbl)中经常发现的温度。由于此处报告的扩散系数和混合时间对应于使用高质量负载产生的SOA(类似于1000μmg(3)),因此在与10μm(3)类似的大气中,在大气中发现的生物学SOA颗粒可能是可能的具有更高的粘度和更长的混合时间(可能是3个数量级)。这些粘度和扩散的新测量用于测试Stokes-Einstein的准确性,以预测棕色LSOA基质内有机物的扩散率。结果表明,当基质的粘度高达10(2)至10(4)时,Stokes-Einstein方程可以精确预测棕色LSOA矩阵内的大型有机物内的大型物体的扩散系数。

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